DOLOTENS DENTAL TM 1— 510(k) K043373

Name: FDA 510(k) clearance K043373
Creator: U.S. Food and Drug Administration
Published: 2005-09-02

Substantially Equivalent

Neuromuscular Technologies, Inc.

FDA 510(k) clearance K043373 for DOLOTENS DENTAL TM 1, Substantially Equivalent on 2005-09-02. Applicant: Neuromuscular Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Neuromuscular Technologies, Inc.
Product code: Code KZM
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 2004-12-08
Decision date: 2005-09-02
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Lake Oswego, OR, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KZM

view all

K161716 — TEETHAN 2.02016-12-21
K130158 — M-SCAN2013-07-25
K113677 — GRINDCARE MEASURE2012-04-05
K082927 — BIOEMG III2009-02-06
K030869 — BITESTRIP2004-05-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.